ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.82123G>A (p.Gly27375Arg)

dbSNP: rs557567114
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
CHEO Genetics Diagnostic Laboratory, Children's Hospital of Eastern Ontario RCV003150703 SCV003838538 uncertain significance Cardiomyopathy 2021-10-12 criteria provided, single submitter clinical testing

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